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1 enting the low intrinsic repair potential of hyaline cartilage.
2 gical development of these distinct types of hyaline cartilage.
3 rogenesis into either permanent or transient hyaline cartilage.
4 has a similar collagen phenotype to that of hyaline cartilage.
5 liably restore the structure and function of hyaline cartilage.
6 promote osteogenic progression of engrafted hyaline cartilage.
7 nt enabled the maintenance of functional and hyaline cartilage.
8 ble of alleviating necrosis at the centre of hyaline cartilage.
10 -bearing unossified epiphyseal and articular hyaline cartilage and for the distal femoral and proxima
11 the long alpha1(IX) transcript expressed in hyaline cartilage and matched the predicted sequence of
12 issues found in a nasal septal biopsy, i.e., hyaline cartilage and perichondrium, for a novel tissue
13 tion of type II collagen is observed in both hyaline cartilages and is secondary to proteoglycan loss
15 -treated cells results in differentiation of hyaline cartilage, and single cell RNAseq analysis ident
16 howed that both MC-Chs and NCC-Chs expressed hyaline cartilage-associated markers and were capable of
17 al type II, IX, and XI collagen phenotype of hyaline cartilage, but the fibrils appear abnormally thi
19 otential and impaired capacity in generating hyaline cartilage, compared to cells isolated from young
20 ar (82 [25%] vs 21 [19%], P = .25); isolated hyaline cartilage defect (77 [23%] vs 20 [18%], P = .29)
21 a culture strategy was developed to engineer hyaline cartilage for engraftment into an acutely damage
24 logy revealed trabecular bones in two cases, hyaline cartilage in another case and a focus of mineral
26 , pigmentation was widespread throughout the hyaline cartilage in either granular composition or as b
29 cartilaginous condylar cartilage, similar to hyaline cartilage in long bones, directly transform into
30 ints showed significantly improved repair of hyaline cartilage in osteochondral defects injected with
31 disc and cartilage is different from that of hyaline cartilage in other diarthrodial joints, and litt
32 dely expressed, but high levels are found in hyaline cartilage in the adult, bone tissue in newborn m
34 MSC sheets' chondrogenic differentiation to hyaline cartilage in vitro via post-contraction cytoskel
37 iated markers and were capable of generating hyaline cartilage-like tissue ectopically and at joint d
38 er at least 21 d, inducing the expression of hyaline cartilage matrix components and anabolic signali
39 maturation of articular chondrocytes in the hyaline cartilage of both developing and degenerated joi
42 The trilaminar appearance depicted within hyaline cartilage on MR images obtained with this sequen
44 tilage survived engraftment and maintained a hyaline cartilage phenotype, but did not form mature art
46 scaffold and exercise treatment experienced hyaline-cartilage regeneration and completely healed car
47 over expression of type X collagen which, in hyaline cartilage structure is not characteristic of the
48 creased subchondral bone formation, improved hyaline-cartilage structure, and good mechanical propert
50 robust method to generate 3D, scaffold-free, hyaline cartilage tissue constructs from hESCs that are
53 by lubrication is fundamental for decreasing hyaline cartilage wear and for maintaining the function
54 cruciate), elastic cartilage, meniscus, and hyaline cartilage were analyzed for NTTPHase activity (t
55 vitro under hypoxia (2.5% O2) produced more hyaline cartilage, which expressed typical articular car
56 jority of vertebrate species have a layer of hyaline cartilage within the fibrous sclera giving an ex